1
CLIA WAIVED multi-CLIN™
Drug Screen Test Device
Instruction Sheet for testing of any combination of the following drugs: AMP/BAR/BZO/COC/THC/MDMA/OPI/
OXY/PCP/PPX/TCA A rapid, one step screening test for the simultaneous, qualitative detection of multiple drugs and drug metabolites in human urine with on-board procedural controls. For professional, in vitro diagnostic use only.
INTENDED USE The multi-CLIN™ Drug Screen Test Device is a lateral flow chromatographic immunoassay for the qualitative detection of multiple drugs and drug metabolites in urine at the following cut-off concentrations listed below. A certificate of waiver is needed for your laboratory in order to run this test. Laboratories with a certificate of waiver must follow the manufacturer’s instructions for performing the test or the test is considered high complexity and is no longer CLIA waived.
Test Calibrator Cut-off Amphetamine (AMP) d-Amphetamine 1,000 ng/mLBarbiturates (BAR) Secobarbital 300 ng/mLBenzodiazepines (BZO) Oxazepam 300 ng/mLCocaine (COC) Benzoylecgonine 300 ng/mLMarijuana (THC) 11-nor-∆9-THC-9 COOH 50 ng/mLMethylenedioxymeth-amphetamine (MDMA)
3,4-Methylenedioxy-methamphetamine 500 ng/mL
Opiates (OPI) Morphine 300 ng/mLOxycodone (OXY) Oxycodone 100 ng/mLPhencyclidine (PCP) Phencyclidine 25 ng/mLPropoxyphene (PPX) Propoxyphene 300 ng/mLTricyclic Anti- depressants (TCA) Nortriptyline 1,000 ng/mL This assay provides only a preliminary analytical test result. A more specific alternate chemical method must be used in order to obtain a confirmed analytical result. Gas chromatography/ mass spectrometry (GC/MS) is the preferred confirmatory method. Clinical consideration and professional judgment should be applied to any drug of abuse test result, particularly when preliminary positive results are indicated.
SUMMARY The multi-CLIN™ Drug Screen Test Device is a rapid urine screening test that can be performed without the use of an instrument. The test utilizes monoclonal antibodies to selectively detect elevated levels of specific drugs in urine. AMPHETAMINE (AMP) Amphetamine is a Schedule II controlled substance available by prescription (Dexedrine®) and is also available on the illicit market. Amphetamines are a class of potent sympathomimetic agents with
therapeutic applications. They are chemically related to the human body’s natural catecholamines: epinephrine and norepinephrine. Acute higher doses lead to enhanced stimulation of the central nervous system and induce euphoria, alertness, reduced appetite, and a sense of increased energy and power. Cardiovascular responses to Amphetamines include increased blood pressure and cardiac arrhythmias. More acute responses produce anxiety, paranoia, hallucinations, and psychotic behavior. The effects of Amphetamines generally last 2-4 hours following use and the drug has a half-life of 4-24 hours in the body. About 30% of Amphetamines are excreted in the urine in unchanged form, with the remainder as hydroxylated and deaminated derivatives. It is also important to note that Amphetamine is a metabolite of Methamphetamine and will appear in the urine of a person who has taken Methamphetamine. d-Methamphetamine, commonly known as crystal”, ice” and “speed”, metabolizes into d-Amphetamine, which will be detected by the Amphetamine (AMP) assay on this device. The multi-CLIN™ Drug Screen Test Device yields a preliminary positive result when the concentration of Amphetamines in urine exceeds 1,000 ng/mL. This is the suggested screening cut-off for positive samples set by the Substance Abuse and Mental Health Services Administration (SAMHSA, USA).1
BARBITURATES (BAR) Barbiturates are central nervous system depressants. They are used therapeutically as sedatives, hypnotics, and anticonvulsants. Barbiturates are almost always taken orally as capsules or tablets. The effects resemble those of intoxication with alcohol. Chronic use of barbiturates leads to tolerance and physical dependence. Short acting Barbiturates taken at 400 mg/day for 2-3 months can produce a clinically significant degree of physical dependence. Withdrawal symptoms experienced during periods of drug abstinence can be severe enough to cause death. Only a small amount (less than 5%) of most Barbiturates are excreted unaltered in the urine. The approximate detection time limits for Barbiturates are: Short acting (e.g. Secobarbital) 100 mg PO (oral) 4.5 daysLong acting (e.g. Phenobarbital) 400 mg PO (oral) 7 days2 The multi-CLIN™ Drug Screen Test Device yields a preliminary positive result when the concentration of Barbiturates in urine exceeds 300 ng/mL. BENZODIAZEPINES (BZO) Benzodiazepines are medications that are frequently prescribed for the symptomatic treatment of anxiety and sleep disorders. They produce their effects via specific receptors involving a neurochemical called gamma aminobutyric acid (GABA). Because they are safer and more effective, Benzodiazepines have replaced barbiturates in the treatment of both anxiety and insomnia. Benzodiazepines are also used as sedatives before some surgical and medical procedures, and for the treatment of seizure disorders and alcohol withdrawal.
EmployeeDrugTestingAce.com
www.EDTAce.comwww.DrugTestingAce.com
Multi-Clin Employee Drug Testing Kits
2
Risk of physical dependence increases if Benzodiazepines are taken regularly (e.g., daily) for more than a few months, especially at higher than normal doses. Stopping abruptly can bring on such symptoms as trouble sleeping, gastrointestinal upset, feeling unwell, loss of appetite, sweating, trembling, weakness, anxiety and changes in perception. Only trace amounts (less than 1%) of most Benzodiazepines are excreted unaltered in the urine; most of the concentration in urine is conjugated drug. The detection period for the Benzodiazepines in urine is 3-7 days. The multi-CLIN™ Drug Screen Test Device yields a preliminary positive result when the concentration of Benzodiazepines in urine exceeds 300 ng/mL. COCAINE (COC) Cocaine is a potent central nervous system (CNS) stimulant and a local anesthetic. Initially, it brings about extreme energy and restlessness while gradually resulting in tremors, over-sensitivity and spasms. In large amounts, cocaine causes fever, unresponsiveness, difficulty in breathing and unconsciousness. Cocaine is often self-administered by nasal inhalation, intravenous injection and free-base smoking. It is excreted in the urine in a short time primarily as Benzoylecgonine.3 Benzoylecgonine, a major metabolite of cocaine, has a longer biological half-life (5-8 hours) than cocaine (0.5-1.5 hours), and can generally be detected for 24-48 hours after cocaine exposure.3 The multi-CLIN™ Drug Screen Test Device yields a preliminary positive result when the concentration of cocaine metabolite in urine exceeds 300 ng/mL. This is the suggested screening cut-off for positive samples set by the Substance Abuse and Mental Health Services Administration (SAMHSA, USA). MARIJUANA (THC) THC (∆9--tetrahydrocannabinol) is the primary active ingredient in cannabis (marijuana). When smoked or orally administered, THC produces euphoric effects. Users have impaired short term memory and slowed learning. They may also experience transient episodes of confusion and anxiety. Long-term, relatively heavy use may be associated with behavioral disorders. The peak effect of marijuana administered by smoking occurs in 20-30 minutes and the duration is 90-120 minutes after one cigarette. Elevated levels of urinary metabolites are found within hours of exposure and remain detectable for 3-10 days after smoking. The main metabolite excreted in the urine is 11-nor-∆9-tetrahydrocannabinol-9-carboxylic acid (∆9-THC-COOH). The multi-CLIN™ Drug Screen Test Device yields a preliminary positive result when the concentration of THC-COOH in urine exceeds 50 ng/mL. This is the suggested screening cut-off for positive samples set by the Substance Abuse and Mental Health Services Administration (SAMHSA, USA).1
METHYLENEDIOXYMETHAMPHETAMINE (MDMA) Methylenedioxymethamphetamine (ecstasy) is a designer drug first synthesized in 1914 by a German drug company for the treatment of obesity. Those who take the drug frequently report adverse effects, such as increased muscle tension and sweating. MDMA is not clearly a stimulant, although it has, in common with amphetamine drugs, a capacity to increase blood pressure and heart rate. MDMA does produce some perceptual changes in the form of increased sensitivity to light, difficulty in focusing, and blurred vision in some users. Its mechanism of action is thought to be via release of the neurotransmitter serotonin. MDMA may also release dopamine, although the general opinion is that this is a secondary effect of the drug. The most pervasive effect of MDMA, occurring in virtually all people who took a reasonable dose of the drug, was to produce a clenching of the jaws.4 The detection period for MDMA in urine is 1-3 days. The multi-CLIN™ Drug Screen Test Device yields a preliminary positive result when the concentration of MDMA in urine exceeds 500 ng/mL. OPIATES (OPI) Opiate refers to any drug that is derived from the opium poppy, including the natural products, morphine and codeine, and the semi-synthetic drugs such as heroin. Opioid is more general, referring to any drug that acts on the opioid receptor. Opioid analgesics comprise a large group of substances which control pain by depressing the central nervous system. Large doses of morphine can produce higher tolerance levels, physiological dependency in users, and may lead to substance abuse. Morphine is excreted unmetabolized, and is also the major metabolic product of codeine and heroin.3 The detection period for opiates in urine is 1-5 days. The multi-CLIN™ Drug Screen Test Device yields a preliminary positive result when the concentration of opiates in urine exceeds 300 ng/mL. OXYCODONE (OXY) Oxycodone is a semi-synthetic opioid with a structural similarity to codeine. The drug is manufactured by modifying thebaine, an alkaloid found in the opium poppy. Oxycodone, like all opiate agonists, provides pain relief by acting on opioid receptors in the spinal cord, brain, and possibly directly in the affected tissues. Oxycodone is prescribed for the relief of moderate to high pain under the well-known pharmaceutical trade names of OxyContin®, Tylox®, Percodan® and Percocet®. While Tylox, Percodan and Percocet contain only small doses of oxycodone hydrochloride combined with other analgesics such as acetaminophen or aspirin, OxyContin consists solely of oxycodone hydrochloride in a time-release form. Oxycodone is known to metabolize by demethylation into oxymorphone and noroxycodone. In a 24-hour urine, 33-61% of a single, 5 mg oral dose is excreted with the primary constituents being unchanged drug (13-19%), conjugated drug (7-29%) and conjugated oxymorphone (13-14%)3. The window of detection for oxycodone in urine is expected to be similar to that of other opioids such as morphine.
3
The multi-CLIN™ Drug Screen Test Device yields a preliminary positive result when the concentration of oxycodone in urine exceeds 100 ng/mL. At present, the Substance Abuse and Mental Health Services Administration (SAMHSA) does not have a recommended screening cutoff for oxycodone positive samples. PHENCYCLIDINE (PCP) Phencyclidine, also known as PCP or Angel Dust, is a hallucinogen that was first marketed as a surgical anesthetic in the 1950’s. It was removed from the market because patients receiving it became delirious and experienced hallucinations. Phencyclidine is used in powder, capsule, and tablet form. The powder is either snorted or smoked after mixing it with marijuana or vegetable matter. Phencyclidine is most commonly administered by inhalation but can be used intravenously, intra-nasally, and orally. After low doses, the user thinks and acts swiftly and experiences mood swings from euphoria to depression. Self-injurious behavior is one of the devastating effects of Phencyclidine. PCP can be found in urine within 4 to 6 hours after use and will remain in urine for 7 to 14 days, depending on factors such as metabolic rate, user’s age, weight, activity, and diet.5 Phencyclidine is excreted in the urine as an unchanged drug (4% to 19%) and conjugated metabolites (25% to 30%).6 The multi-CLIN™ Drug Screen Test Device yields a preliminary positive result when the concentration of phencyclidine in urine exceeds 25 ng/mL. This is the suggested screening cut-off for positive samples set by the Substance Abuse and Mental Health Services Administration (SAMHSA, USA). PROPOXYPHENE (PPX) Propoxyphene is a narcotic analgesic compound bearing structural similarity to methadone. Darvocet™, one of the most common brand names for the drug, contains 50-100 mg of propoxyphene napsylate and 325-650 mg of acetaminophen. After a typical 100 mg oral dose of propoxyphene napsylate, peak plasma concentrations of 0.05 µg/mL to 0.1 µg/mL are achieved from 2 to 2½ hours post dose. Repeat doses of propoxyphene at 6-hour intervals leads to increasing plasma concentrations, with a plateau after the ninth dose at 48 hours. In the case of overdose, propoxyphene blood concentrations can reach significantly higher levels. Propoxyphene is metabolized in the liver to yield norpropoxyphene. Norpropoxyphene has a longer half-life (30 to 36 hours) than parent propoxyphene (6 to 12 hours).5 The multi-CLIN™ Drug Screen Test Device yields a preliminary positive result when the concentration of Propoxyphene or Norpropoxyphene in urine exceeds 300 ng/mL. At present, the Substance Abuse and Mental Health Services Administration (SAMHSA) does not have a recommended screening cutoff for propoxyphene positive samples.
TRICYCLIC ANTIDEPRESSANTS (TCA) TCA (Tricyclic Antidepressants) are commonly used for the treatment of depressive disorders. TCA overdoses can result in profound central nervous system depression, cardiotoxicity and anticholinergic effects. TCA overdose is the most common cause of death from prescription drugs. TCAs are taken orally or sometimes by injection. TCAs are metabolized in the liver. Both TCAs and their metabolites are excreted in urine mostly in the form of metabolites for up to ten days. The multi-CLIN™ Drug Screen Test Device yields a preliminary positive result when the concentration of Tricyclic Antidepressants in urine exceeds 1,000 ng/mL.
PRINCIPLE The multi-CLIN™ Drug Screen Test Device is an immunoassay based on the principle of competitive binding. Drugs which may be present in the urine sample compete against their respective drug conjugate for binding sites on their specific antibody. During testing, a urine sample migrates upward by capillary action. A drug, if present in the urine sample below its cut-off concentration, will not saturate the binding sites of its specific antibody. The antibody will then react with the drug-protein conjugate and a visible colored line will show up in the test line region of the specific drug strip. The presence of drug above the cut-off concentration will saturate all the binding sites of the antibody. Therefore, the colored line will not form in the test line region. A drug-positive urine sample will not generate a colored line in the specific test line region of the strip because of drug competition, while a drug-negative urine sample will generate a line in the test line region because of the absence of drug competition.
Internal Procedural Controls To serve as an internal procedural control, the test includes both a Positive and Negative Control Region.
Positive Control When the test is manufactured, an antigen-BSA conjugate is striped in the Positive Control Region (POS) with a water-soluble blue dye as a visual marker. The positive control antigen is included in the label pad. When the test is run properly, the migration of the sample will make this blue line disappear. Therefore, the absence of a line in the Positive Control Region (POS) serves as an internal positive procedural control. The presence of a blue line in the Positive Control Region (POS) could indicate that an immunochemical reaction did not occur and the results should be considered invalid.
Negative Control A line in the Negative Control Region (NEG) confirms that proper volume of sample has been added and membrane wicking has occurred. There must be a line present in the Negative Control Region (NEG) for the test results to be valid.
4
The absence of a Positive Control line confirms the internal procedural control and, along with the appearance of the Negative Control line, the validity of the test results. If the test is working properly, a line should always appear in the Negative Control Region (NEG) and NO line should appear in the Positive Control Region (POS).
REAGENTS Each test line contains anti-drug mouse monoclonal antibody and corresponding drug-protein conjugates. Control line contains goat anti-rabbit IgG polyclonal antibodies and rabbit IgG.
PRECAUTIONS • For professional, in vitro diagnostic use only. • Do not use after the expiration date. • The test device should remain in the sealed pouch
until use. • All samples should be considered potentially
hazardous and handled in the same manner as an infectious agent.
• The used test device should be discarded according to federal, state and local regulations
• Color blindness may affect interpretation of results. STORAGE AND STABILITY
Store as packaged in the sealed pouch at 2-30°C. The test device is stable through the expiration date printed on the sealed pouch. The test device must remain in the sealed pouch until use. DO NOT FREEZE. Do not use beyond the expiration date.
SAMPLE COLLECTION AND PREPARATION Urine Assay
The urine sample must be collected in a clean and dry container. Urine collected at any time of the day may be used. Do not use cloudy samples or urine samples with visible precipitates for testing.
Sample Storage Urine samples may be stored at 2-8°C for up to 48 hours prior to testing. For prolonged storage, samples may be frozen and stored below -20°C. Frozen samples should be thawed and mixed well before testing.
MATERIALS Materials Provided
• Test devices • Disposable droppers • Package insert • Procedure card
Materials Required But Not Provided • Sample collection container • Timer • Positive and Negative Controls
DIRECTIONS FOR USE
Allow test device and urine sample to reach room temperature (15-30°C) before testing. 1. Remove the test device from the sealed pouch. Use
it as soon as possible. 2. Place the test device on a clean and level surface.
Add 100 µL of urine (3 full drops using the included pipette) to each of the sample wells of the test device. [See image (1).] Start the timer. Avoid trapping air bubbles in the sample well.
3. Wait for the colored lines(s) to appear. [See image (2).] The results should be read at 5 minutes. Test results will be stable for at least 8 hours after test initiation.
RESULT INTERPRETATION [Please refer to image (4).]
First, confirm the validity of the results by reviewing the Negative and Positive Control Lines. If there is a line in the Positive Control Region (POS), the result is INVALID. There must be a line in the Negative Control Region (NEG) for the result to be VALID. Before interpreting testing results, make sure that there is no line next to “POS” and a visible line next to “NEG”. [See image (3).] NEGATIVE RESULT:* A colored line appears in the Negative Control region (NEG), no line appears in the Positive Control Region (POS) and a colored line appears in the Test region next to a specific drug tested. Up to four colored lines may appear in each result window. One line will be in the Negative Control region (NEG). Up to three lines will be next to the drug names in the Test region. This negative result means that the drug concentration in the urine sample is below the detectable level for a certain drug tested. *NOTE: The shade of the colored line(s) in the Test region may vary. The result should be considered negative when there is even a faint color line. PRELIMINARY POSITIVE RESULT: A colored line appears in the Negative Control region (NEG), no line appears in the Positive Control Region (POS) and NO line appears in the Test region next to the name of a certain drug tested. The preliminary positive result means that the drug concentration in the urine sample is greater than the detectable level for a certain drug tested. INVALID: No line appears in the Negative Control region (NEG) and/or a line appears in the Positive Control Region (POS). Not enough sample volume or incorrect procedural techniques are the most likely reasons for an invalid result. Review the directions for use and repeat the test with a new test device. If the problem continues, contact Technical Service.
5
QUALITY CONTROL
Internal Quality Control A procedural control is included in the test. The presence of a red line in the Negative Control region (NEG) and the absence of a line in the Positive Control Region (POS) are considered internal procedural controls. This confirms sufficient sample volume, adequate membrane wicking and correct procedural technique.
The internal procedural controls contained within the device satisfy the daily control testing requirement provided they are used in conjunction with a comprehensive laboratory Quality Assurance program.
External Quality Control It is recommended that external positive and negative controls be tested with each new lot or shipment of product, with each change in operator within the test kit, weekly as a check on continued storage conditions, or as otherwise required by your laboratory’s internal quality system procedures.
External Positive and Negative Controls are available separately. Please contact your distributor for a list of approved controls that have been validated with the multi-CLIN™ Drug Screen Test Device. Use of any other control material is not advised and could produce irregular results. If unexpected results are seen when running the controls, review the Directions for Use, Interpretation of Results and Limitations sections and repeat the test with another device. If the problem persists, discontinue use of the test kit immediately and contact the manufacturer at 858-535-2030. CLIA waived laboratories must follow the manufacturer’s instructions for quality control testing.
INVALIDRESULTS
NEGAMPCOCTHCPOS
NEGAMPCOCTHCPOS
VALID RESULT, NEGATIVE for
ALL ANALYTES SHOWN
VALID RESULT, PRELIMINARY
POSITIVE for COC
NEGAMPCOCTHCPOS
VALID RESULT, PRELIMINARY POSITIVE for
ALL ANALYTES SHOWN
NEGAMPCOCTHCPOS
Interpret results at 5 minutes.
4
Confirm validity of results by checking NEG and POS Control Regions.There should be NO line in the Positive Control Region (POS) and a visible line in the Negative Control Region (NEG).
3
NEGAMPCOCTHCPOS
EXAMPLES OFVALID RESULTS
NEGAMPCOCTHCPOS
NEGAMPCOCTHCPOS
NEGBZOTCABARPOS
NEGMDMAOPIPCPPOS
NEGOXYPPX
POS
NEG
POS
NEG
POS
NEG
POS
NEG
POS
VALID RESULT
INVALID RESULT
INVALID RESULT
INVALID RESULT
IDDATE
NEGAMPCOCTHCPOS
2
Wait 5 minutes to read results.
NEG
BZO
TCA
BA
RPO
S
NEG
MDM
AO
PIPC
PPO
S
NEG
OXY
PPX
POS
NEG
POS
NEG
POS
NEG
POS
NEG
POS
VALID
R
ES
ULT
INVA
LID
RE
SU
LTIN
VALID
R
ES
ULT
INVA
LID
RE
SU
LT
IDDATE
NEG
AM
PC
OC
THC
POS
Add 100 µL of urine(3 drops using pipette) to EACH sample well.
1
6
LIMITATIONS
1. The multi-CLIN™ Drug Screen Test Device provides only a qualitative, preliminary analytical result. A secondary analytical method must be used to obtain a confirmed result. Gas chromatography/ mass spectrometry (GC/MS) is the preferred confirmatory method.1
2. There is a possibility that clinical, technical or procedural errors, as well as other interfering substances in the urine sample may cause erroneous results.
3. Adulterants, such as bleach and/or alum, in urine samples may produce erroneous results regardless of the analytical method used. If adulteration is suspected, the test should be repeated with another urine sample.
4. A preliminary positive result does not indicate level of intoxication, administration route or concentration in urine.
5. A negative result may not necessarily indicate drug-free urine. Negative results can be obtained when drug is present but below the cut-off level of the test.
6. Test does not distinguish between drugs of abuse and certain medications.
7. A preliminary positive test result might be obtained from certain foods or food supplements.
PERFORMANCE CHARACTERISTICS
Accuracy A side-by-side comparison was conducted using the multi-CLIN™ Drug Screen Test Device and commercially available drug rapid tests. Testing was performed on 1,704 samples previously collected from subjects presenting for Drug Screen Testing. Preliminary positive results were confirmed by GC/MS. Negative urine samples were screened initially by Predicate test. The following compounds were quantified by GC/MS and contributed to the total amount of drugs found in preliminary positive urine samples tested in the following clinical studies:
Test Compounds Contributing to the Totals of GC/MSAMP Amphetamine BAR Secobarbital, Butalbital, Phenobarbital, Pentobarbital
BZO Oxazepam, Nordiazepam, Alprazolam, α-OH, Desalkylflurazepam
COC Benzoylecgonine THC 11-nor-∆9-tetrahydrocannabinol-9-carboxylic acid
MDMA 3,4-Methylenedioxymethamphetamine, Methylenedioxyamphetamine
OPI Morphine, Codeine OXY Oxycodone PCP Phencyclidine PPX Propoxyphene TCA Nortriptyline
The following results were tabulated:
Method GC/MS
Neg
ativ
e*
Neg
ativ
e
(<-2
5% c
utof
f)
Nea
r cut
off
Neg
ativ
e (-2
5%
cuto
ff to
cut
off)
Nea
r cut
off
Pos
itive
(cut
off
to +
25%
cut
off)
Pos
itive
(>
+25%
cut
off)
% a
gree
men
t w
ith G
C/M
S
+ 0 0 6 20 114AMP- 300 2 6 2 0
98%
+ 0 1 3 3 96 BAR- 300 0 5 1 1
99%
+ 0 1 1 3 136BZO- 300 2 6 1 0
>99%
+ 0 2 15 14 105COC- 300 3 5 0 0
96%
+ 0 9 7 11 105THC- 300 9 2 3 2
95%
+ 0 0 4 6 82 MDMA- 300 0 1 0 0
99%
+ 0 2 7 10 130OPI- 300 0 0 0 0
98%
+ 0 1 2 2 138OXY- 300 2 4 1 0
99%
+ 0 4 0 11 74 PCP- 300 0 0 1 0
99%
+ 0 0 0 2 143PPX- 300 0 4 1 0
>99%
+ 0 13 9 14 18 TCA**- 300 16 0 0 0
94%
* Negative urine samples were screened by predicate
tests and approximately 10% were confirmed negative by GC/MS.
**Note: TCA concentration was based on HPLC data.
Predicate Test Results Method
Pos. Neg.
% Agreement with Predicate
Test Pos. 140 0 AMP Neg. 3 307 >99%
Pos. 103 0 BAR Neg. 0 307 >99%
Pos. 122 1 BZO Neg. 0 302 >99%
Pos. 132 4 COC Neg. 0 308
99%
Pos. 132 0 THC Neg. 9 307 98%
Pos. 91 1 MDMA Neg. 0 301 >99%
Pos. 149 0 OPI Neg. 0 300 >99%
Pos. 141 2 OXY Neg. 0 307
>99%
Pos. 89 0 PCP Neg. 0 301
>99%
Pos. 135 0 PPX Neg. 0 305
>99%
Pos. 54 0
mul
ti-C
LIN
™
Dru
g Sc
reen
Tes
t Dev
ice
TCA Neg. 0 316
>99%
7
Analytical Sensitivity A drug-free urine pool was spiked with drugs to various concentrations. >99% agreement with expected results was found at ± 50% cut-off for each drug tested (with a 95% confidence interval).
Analytical Specificity The following table lists the concentration of compounds (ng/mL) that are detected as preliminary positives in urine by the multi-CLIN™ Drug Screen Test Device at 5 minutes. Compound ng/mL AMPHETAMINE d-Amphetamine 1,000 d,l-Amphetamine 3,000 l-Amphetamine 50,000 p-Hydroxyamphetamine 3,125 3,4-Methylenedioxyamphetamine (MDA) 2,000 Phentermine 3,000
BARBITURATES Secobarbital 300 Amobarbital 300 Alphenol 150 Aprobarbital 200 Butabarbital 75 Butalbital 2,500 Butethanol 100 Cyclobarbital 400 Cyclopentobarbital 600 Pentobarbital 300 Phenobarbital 100
BENZODIAZEPINES Oxazepam 300 Alprazolam 196 Alprazolam, α-OH 1,262 Bromazepam 1,562 Chlordiazepoxide 1,562 Clobazam 98 Clonazepam 781 Clorazepate 195 Delorazepam 1,562 Desalkylflurazepam 390 Diazepam 195 Estazolam 2,500 Flunitrazepam 390 (±) Lorazepam 1,562 RS-Lorazepam glucuronide 156 Midazolam 12,500 Nitrazepam 98 Norchlordiazepoxide 195 Nordiazepam 390 Temazepam 98 Triazolam 2,500
COCAINE Benzoylecgonine 300 Cocaine 780 Cocaethylene 12,500 Ecgonine 32,000
MARIJUANA (THC) 11-nor-∆9 -THC-9 COOH 50 Cannabinol 20,000
Compound ng/mL 11-nor-∆8-THC-9 COOH 30 ∆8 -THC 15,000 ∆9 -THC 15,000
METHYLENEDIOXYMETHAMPHETAMINE 3,4-Methylenedioxymethamphetamine (MDMA) 500 l-Methamphetamine 100,000 3,4-Methylenedioxyamphetamine (MDA) 3,000 3,4-Methylenedioxyethylamphetamine (MDEA) 300
OPIATE 300 (OPI) Morphine 300 Codeine 300 Ethylmorphine 6,250 Hydrocodone 50,000 Hydromorphone 3,125 Levorphanol 1,500 6-Monoacetylmorphine 400 Morphine 3-β-d-glucuronide 1,000 Norcodeine 6,250 Normorphone 100,000 Oxycodone 30,000 Oxymorphone 100,000 Thebaine 6,250
OXYCODONE Oxycodone 100 6-Acetylcodeine 100,000 Codeine 25,000 Dihydrocodeine 12,500 Ethylmorphine 25,000 Hydrocodone 6,250 Hydromorphone 12,500 Levorphanol 100,000 6-Monoacetylmorphine 100,000 Morphine 100,000 Morphine 3-β-d-glucuronide 100,000 Norcodeine 100,000 Normorphone 100,000 Oxymorphone 780 Procaine 100,000 Thebaine 25,000 PHENCYCLIDINE Phencyclidine 25 4-Hydroxyphencyclidine 12,500
PROPOXYPHENE d-Propoxyphene 300 Norpropoxyphene 300
TRICYCLIC ANTIDEPRESSANTS Nortriptyline 1,000 Amitriptyline 1,500 Clomipramine 12,500 Cyclobenzaprine 6,250 Desipramine 200 Doxepin 2,000 Imipramine 400 Maprotiline 2,000 Nordoxepin 1,000 Perphenazine 50,000 Promazine 1,500 Promethazine 25,000 Trimipramine 3,000
8
CLIA Waiver Performance
A total of 75 untrained, inexperienced, non-laboratory participants were enrolled at three separate locations to demonstrate that they could follow the product instructions and perform the multi-CLIN™ Drug Screen Test Device and obtain results similar to the expected results determined by GC/MS. Each participant received seven blinded spiked urine samples (one sample for each of following spiked solutions: invalid, negative, -50% of cutoff, -25% of cutoff, +25% of cutoff, +50% of cutoff and +200% of cutoff). Study participants followed the Package Insert and Procedure Card instructions to test the provided samples and recorded their test results. No other instruction or training was given. Upon completion of the test, participants filled out a brief questionnaire regarding the test procedure and ease of use of the labeling. The user study data confirmed that the untrained study participants are able to read the test endpoint with a high degree of precision as compared to the expected results determined by GC/MS. The results were summarized and tabulated as follows:
Agreement (%) - Test Results from Untrained Participants
vs. GC/MS Data AMP Conc. Site 1 Site 2 Site 3
Negative 25/25 > 99% 25/25 > 99% 25/25 > 99%-50% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%-25% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%+25% of Cutoff 22/25 = 88% 24/25 = 96% 24/25 = 96%+50% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%+200% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%
Invalid 25/25 > 99% 25/25 > 99% 25/25 > 99%Total Correct 172/175 = 98%
(95%-99%)* 174/175 = 99%
(97%-99%)* 174/175 = 99%
(97%-99%)* * Denotes 95% Confidence Intervals
Agreement (%) - Test Results from Untrained Participants
vs. GC/MS Data COC Conc. Site 1 Site 2 Site 3
Negative 25/25 > 99% 25/25 > 99% 25/25 > 99%-50% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%-25% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%+25% of Cutoff 22/25 = 88% 24/25 = 96% 24/25 = 96%+50% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%+200% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%
Invalid 25/25 > 99% 25/25 > 99% 25/25 > 99%Total Correct 172/175 = 98%
(95%-99%)* 174/175 = 99%
(97%-99%)* 174/175 = 99%
(97%-99%)* * Denotes 95% Confidence Intervals
Agreement (%) - Test Results from Untrained Participants
vs. GC/MS Data THC Conc. Site 1 Site 2 Site 3
Negative 25/25 > 99% 25/25 > 99% 25/25 > 99%-50% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%-25% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%+25% of Cutoff 24/25 = 96% 24/25 = 96% 24/25 = 96%+50% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%+200% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%
Invalid 25/25 > 99% 25/25 > 99% 25/25 > 99%Total Correct 174/175 = 99%
(97%-99%)* 174/175 = 99%
(97%-99%)* 174/175 = 99%
(97%-99%)* * Denotes 95% Confidence Intervals
Agreement (%) - Test Results from
Untrained Participants vs. GC/MS Data BZO Conc.
Site 1 Site 2 Site 3 Negative 25/25 > 99% 25/25 > 99% 25/25 > 99%
-50% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%-25% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%+25% of Cutoff 20/25 = 80% 23/25 = 92% 24/25 = 96%+50% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%+200% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%
Invalid 25/25 > 99% 25/25 > 99% 25/25 > 99%Total Correct 170/175 = 97%
(93%-99%)* 173/175 = 99%
(96%-99%)* 174/175 = 99%
(97%-99%)* * Denotes 95% Confidence Intervals
Agreement (%) - Test Results from Untrained Participants
vs. GC/MS Data TCA Conc. Site 1 Site 2 Site 3
Negative 25/25 > 99% 25/25 > 99% 25/25 > 99%-50% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%-25% of Cutoff 24/25 = 96% 25/25 > 99% 25/25 > 99%+25% of Cutoff 20/25 = 80% 23/25 = 92% 24/25 = 96%+50% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%+200% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%
Invalid 25/25 > 99% 25/25 > 99% 25/25 > 99%Total Correct 169/175 = 97%
(93%-99%)* 173/175 = 99%
(96%-99%)* 174/175 = 99%
(97%-99%)* * Denotes 95% Confidence Intervals
Agreement (%) - Test Results from Untrained Participants
vs. GC/MS Data BAR Conc. Site 1 Site 2 Site 3
Negative 25/25 > 99% 25/25 > 99% 25/25 > 99%-50% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%-25% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%+25% of Cutoff 20/25 = 80% 23/25 = 92% 24/25 = 96%+50% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%+200% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%
Invalid 25/25 > 99% 25/25 > 99% 25/25 > 99%Total Correct 170/175 = 97%
(93%-99%)* 173/175 = 99%
(96%-99%)* 174/175 = 99%
(97%-99%)* * Denotes 95% Confidence Intervals
Agreement (%) - Test Results from Untrained Participants
vs. GC/MS Data MDMA Conc. Site 1 Site 2 Site 3
Negative 25/25 > 99% 25/25 > 99% 25/25 > 99%-50% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%-25% of Cutoff 25/25 > 99% 25/25 > 99% 24/25 = 96%+25% of Cutoff 21/25 = 84% 25/25 > 99% 24/25 = 96%+50% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%+200% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%
Invalid 25/25 > 99% 25/25 > 99% 25/25 > 99%Total Correct 171/175 = 98%
(94%-99%)* 175/175 > 99%
(98%-99%)* 173/175 = 99%
(96%-99%)* * Denotes 95% Confidence Intervals
Agreement (%) - Test Results from Untrained Participants
vs. GC/MS Data OPI Conc. Site 1 Site 2 Site 3
Negative 25/25 > 99% 25/25 > 99% 25/25 > 99%-50% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%-25% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%+25% of Cutoff 20/25 = 80% 24/25 = 96% 25/25 > 99%+50% of Cutoff 23/25 = 92% 25/25 > 99% 25/25 > 99%+200% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%
Invalid 25/25 > 99% 25/25 > 99% 25/25 > 99%Total Correct 168/175 = 96%
(92%-98%)* 174/175 = 99%
(97%-99%)* 175/175 > 99%
(98%-99%)* * Denotes 95% Confidence Intervals
9
Agreement (%) - Test Results from
Untrained Participants vs. GC/MS Data PCP Conc.
Site 1 Site 2 Site 3 Negative 25/25 > 99% 25/25 > 99% 25/25 > 99%
-50% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%-25% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%+25% of Cutoff 24/25 = 96% 25/25 > 99% 25/25 > 99%+50% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%+200% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%
Invalid 25/25 > 99% 25/25 > 99% 25/25 > 99%Total Correct 174/175 = 99%
(97%-99%)* 175/175 > 99%
(98%-99%)* 175/175 > 99%
(98%-99%)* * Denotes 95% Confidence Intervals
Agreement (%) - Test Results from Untrained Participants
vs. GC/MS Data OXY Conc. Site 1 Site 2 Site 3
Negative 25/25 > 99% 25/25 > 99% 25/25 > 99%-50% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%-25% of Cutoff 23/25 = 92% 25/25 > 99% 24/25 = 96%+25% of Cutoff 23/25 = 92% 24/25 = 96% 24/25 = 96%+50% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%+200% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%
Invalid 25/25 > 99% 25/25 > 99% 25/25 > 99%Total Correct 171/175 = 98%
(94%-99%)* 174/175 = 99%
(97%-99%)* 173/175 = 99%
(96%-99%)* * Denotes 95% Confidence Intervals
Agreement (%) - Test Results from Untrained Participants
vs. GC/MS Data PPX Conc. Site 1 Site 2 Site 3
Negative 25/25 > 99% 25/25 > 99% 25/25 > 99%-50% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%-25% of Cutoff 22/25 = 88% 25/25 > 99% 25/25 > 99%+25% of Cutoff 22/25 = 88% 24/25 = 96% 25/25 > 99%+50% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%+200% of Cutoff 25/25 > 99% 25/25 > 99% 25/25 > 99%
Invalid 25/25 > 99% 25/25 > 99% 25/25 > 99%Total Correct 169/175 = 97%
(93%-99%)* 174/175 = 99%
(97%-99%)* 175/175 > 99%
(98%-99%)* * Denotes 95% Confidence Intervals
Precision A study was conducted at three physician offices for Amphetamine, Barbiturates, Benzodiazepines, Cocaine, Marijuana, Methylenedioxymethamphetamine, Opiates, Oxycodone, Phencyclidine, Propoxyphene and Tricyclics by untrained operators using three different lots of product to demonstrate the within run, between run and between operator precision. An identical panel of coded samples, containing drugs at the concentration of ± 50% cut-off level was labeled as a blind and tested at each site. The correlation with expected results was >99% across all lots and sites (with a 95% confidence interval).
Effect of Urinary Specific Gravity Urine samples of low, normal and high specific gravity (1.004-1.034) were spiked with drugs at ± 50% cut-off levels and analyzed. The results demonstrate that varying ranges of urinary specific gravity do not affect the test results.
Effect of Urinary pH Urine samples with pH ranges from 5-9 in 1 pH unit increments were spiked with drugs at ± 50% cut-off levels and analyzed. The results demonstrate that varying ranges of pH (5-9) do not interfere with the performance of the test.
Cross-Reactivity
A study was conducted to determine the cross-reactivity of the test with compounds in either drug-free urine or Amphetamine, Barbiturates, Benzodiazepines, Cocaine, Marijuana, Methylenedioxymethamphetamine, Opiates, Oxycodone, Phencyclidine, Propoxyphene and Tricyclic positive urine. The following compounds show no cross-reactivity when tested with the multi-CLIN™ Drug Screen Test Device at a concentration of 100 µg/mL.
Non-Cross Reacting Compounds Acetaminophen Acetone Acetophenetidin N-Acetylprocainamide Acetylsalicylic acid Albumin Albuterol Aminopyrine Amoxapine Amoxicillin Ampicillin Apomorphine l-Ascorbic acid Aspartame Atropine Baclofen Benzilic acid Benzocaine Benzoic acid Benzphetamine* Bilirubin d/l-Brompheniramine Buprenorphine Buspirone Caffeine Cannabidiol Carisoprodol Chloralhydrate Chloramphenicol Chloroquine Chlorothiazide d/l-Chlorpheniramine Chlorpromazine Chlorpropamide Chlorprothixene Cholesterol Cimetidine Clonidine Clozapine Cortisone l-Cotinine Creatinine Deoxycorticosterone R(-)Deprenyl Dextromethorphan Diclofenac Dicyclomine Diflunisal Digitoxin Digoxin (+)-cis-Diltiazem Dimenhydrinate 4-Dimethylaminoantipyrine Diphenhydramine 5,5-Diphenylhydantoin Disopyramide Dopamine Doxylamine Droperidol Ecgonine methyl ester EDDP Efavirenz* EMDP Ephedrine l-Ephedrine [1R,2S](-)Ephedrine l-Epinephrine (±)Epinephrine Erythromycin β-Estradiol Estrone-3-sulfate Ethanol (Ethyl alcohol) Ethyl-p-aminobenzoate Etodolac Famprofazone Fenfluramine Fenoprofen Fentanyl Fluoxetine Furosemide Gentamicin Gentisic acid d(+)Glucose Guaiacol Glyceryl Ether Haloperidol Hemoglobin Hydralazine Hydrochlorothiazide Hydrocortisone o-Hydroxyhippuric acid p-Hydroxymethamphetamine p-Hydroxynorephedrine Hydroxyzine Ibuprofen Indomethacin Insulin Iproniazid l-Isoproterenol Isoxsuprine Kanamycin Ketamine Ketoprofen Labetalol Lidocaine Lindane Lithium Loperamide Meperidine Mephentermine Meprobamate Methadone d-Methamphetamine Methaqualone Methoxyphenamine Methylphenidate Methyprylon Metoprolol Metronidazole Nalidixic acid Nalorphine Naloxone Naltrexone α-Naphthaleneacetic Acid Naproxen Niacinamide Nifedipine Nimesulide Norethindrone
10
Norfluoxetine Noscapine d/l-Octopamine Orphenadrine Oxalic acid Oxolinic acid Oxymetazoline Papaverine Pemoline Penicillin-G Pentazocine Phenelzine Pheniramine Phenothiazine Trans-2-phenylcyclopropylamine l-Phenylephrine β-Phenylethylamine Phenylpropanolamine (±) Phenylpropanolamine (d/l-Norephedrine) Prednisolone Prednisone 5-β-pregnane-3α, 17α, 21-triol-20-one Procaine d/l-Propranolol d-Pseudoephedrine Quinacrine Quinine Quindine Ranitidine Riboflavin Salbutamol Salicylic acid Serotonin Sodium chloride Spironolactone Sulfamethazine Sulfamethoxazole Sulfisoxazole Sulindac Tetracycline Tetrahydrocortisone 3-acetate Tetrahydrozoline Theophylline Thiamine Thioridazine Thiothixene l-Thyroxine Tobramycin Tolbutamide Tramadol Trazodone Trimethobenzamide Triamterene Trifluoperazine Trimethoprim Tryptamine d/l-Tryptophan Tyramine d/l-Tyrosine Uric acid Verapamil Zomepirac Zopiclone *Parent compound only
BIBLIOGRAPHY
1. Procedures for Transportation Workplace Drug and Alcohol Testing Programs, 49 CFR 40. Reprinted by the Department of Transportation, Drug and Alcohol Policy and Compliance Office, 400 7th St., SW, Washington, DC 20590, (202) 366-3784.
2. Tietz NW. Textbook of Clinical Chemistry. W.B. Saunders Company. 1986, 1734.
3. Baselt R. Disposition of Toxic Drugs and Chemicals in Man, 6th Ed. Biomedical Publications. 2002.
4. Climko RP. Ecstacy: A Review of MDMA and MDA. Int’l J Psychiatry in Medicine. 16(4); 1986-1987, 359-372.
5. Hardman J, Limbird LE (Eds). Goodman & Gilman’s The Pharmacological Basis of Therapeutics, 10th Ed., McGraw-Hill Publishing. 2001, 598.
CLIA Category: Waived
Distributed by Innovacon, Inc., San Diego, CA 92121
DN: 1155288602
Eff. Date: 2006-10-25
Printed in China
http://www.employee-drug-testing-ace.com/employment-drug-screening-resources/employee-drug-screening-and-testing-library
© Copyright Employee Drug Testing Ace
www.EDTAce.coma.k.a. www.DrugTestingAce.coma.k.a.
Trusted Proven SecureEmployeeDrugTestingAce.com
Brought to You by Employee Drug Testing Ace Buying discounted, accurate, high quality employment drug testing kits and services is affordable, fast, easy, safe and secure with Employee Drug Testing Ace. You can buy employment, pre-employment and employee drug and alcohol testing kits, services and supplies tailored for employers, TPAs, nursing homes, hospitals, manufacturing, moving companies, Department of Transportation DOT, local and Federal Government agencies, auto dealerships, construction, DOD, the work place, employment agencies and more. Our easy to use employee drug testing kits are DOT Approved, CLIA Waived, FDA 510k Cleared and SAMHSA Compliant. We provide both onsite employment drug screening and offsite employee drug screening services along with SAMHSA certified confirmation and medical review officer (MRO) services. All employment drug screening kits are on sale, discounted, and have bulk / volume discounts.
• Pay No Taxes in the USA., except California.
• 100% Free UPS Standard Shipping in the Continental U.S.A. for All Products.
• 100% Free FedEx Overnight Shipping in the Continental U.S.A. for All Specimens sent in as part of our SAMHSA Certified Confirmation Drug Testing Service.
• Onsite Third Party Administered (TPA) Employee Drug and Alcohol Collection Services.
• Over 12,000 Offsite Employee Drug and Alcohol Testing Locations Nationwide.
• The most complete Employment Drug Testing Resource Center including: information, official documents, work place drug testing information, forms, work accident info, charts, videos, post accident drug testing info, training materials, contact lists, definitions and more!
We sell affordable and guaranteed employee drug screening kits and services available at the best prices. Our prices may be cheap but our drug testing kits are of the highest quality and accuracy. If you are in the market for discounted high quality pre-employment, employee, or employment drug testing and screening kits and services, visit us today. You will be happy you did!